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dc.contributor.authorBarrett, M. F.
dc.contributor.authorWerpy, N. M.
dc.contributor.authorMcIlwraith, C. Wayne
dc.contributor.authorFrisbie, David D.
dc.contributor.authorGrodzinsky, Alan J.
dc.contributor.authorHung, Han-Hwa K.
dc.contributor.authorFrank, Eliot
dc.contributor.authorMiller, Rachel Elizabeth
dc.date.accessioned2014-10-14T19:46:13Z
dc.date.available2014-10-14T19:46:13Z
dc.date.issued2014-10
dc.identifier.issn0021-9355
dc.identifier.issn1535-1386
dc.identifier.urihttp://hdl.handle.net/1721.1/90920
dc.description.abstractBackground: The goal of this study was to test the ability of an injectable self-assembling peptide (KLD) hydrogel, with or without microfracture, to augment articular cartilage defect repair in an equine cartilage defect model involving strenuous exercise. Methods: Defects 15 mm in diameter were created on the medial trochlear ridge and debrided down to the subchondral bone. Four treatment groups (n = 8 each) were tested: no treatment (empty defect), only defect filling with KLD, only microfracture, and microfracture followed by filling with KLD. Horses were given strenuous exercise throughout the one-year study. Evaluations included lameness, arthroscopy, radiography, and gross, histologic, immunohistochemical, biochemical, and biomechanical analyses. Results: Overall, KLD-only treatment of defects provided improvement in clinical symptoms and improved filling compared with no treatment, and KLD-only treatment protected against radiographic changes compared with microfracture treatment. Defect treatment with only microfracture also resulted in improved clinical symptoms compared with no treatment, and microfracture treatment resulted in repair tissue containing greater amounts of aggrecan and type-II collagen compared with KLD-only treatment. Microfracture treatment also protected against synovial fibrosis compared with no treatment and KLD-only treatment. Treatment with the self-assembling KLD peptide in combination with microfracture resulted in no additional improvements over microfracture-only treatment. In general, the nature of the predominant tissue in the defects was a mix of noncartilaginous and fibrocartilage tissue, with no significant differences among the treatments. Conclusions: Treatment of defects with only KLD or with only microfracture resulted in an improvement in clinical symptoms compared with no treatment; the improvement likely resulted from different causes depending on the treatment. Whereas microfracture improved the quality of repair tissue, KLD improved the amount of filling and protected against radiographic changes. Clinical Relevance: Treatment of defects with only microfracture and with KLD only resulted in clinical improvements compared with untreated defects, despite differing with respect to the structural improvements that they induced.en_US
dc.language.isoen_US
dc.publisherJournal of Bone and Joint Surgery, Incen_US
dc.relation.isversionofhttp://dx.doi.org/10.2106/jbjs.m.01408en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceJournal of Bone and Joint Surgery, Inc.en_US
dc.titleEffects of the Combination of Microfracture and Self-Assembling Peptide Filling on the Repair of a Clinically Relevant Trochlear Defect in an Equine Modelen_US
dc.typeArticleen_US
dc.identifier.citationMiller, R. E., A. J. Grodzinsky, M. F. Barrett, H.-H. Hung, E. H. Frank, N. M. Werpy, C. W. McIlwraith, and D. D. Frisbie. “Effects of the Combination of Microfracture and Self-Assembling Peptide Filling on the Repair of a Clinically Relevant Trochlear Defect in an Equine Model.” The Journal of Bone & Joint Surgery 96, no. 19 (October 1, 2014): 1601–1609. © 2014 by The Journal of Bone and Joint Surgery, Incorporateden_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.mitauthorGrodzinsky, Alan J.en_US
dc.contributor.mitauthorHung, Han-Hwa K.en_US
dc.contributor.mitauthorFrank, Elioten_US
dc.contributor.mitauthorMiller, Rachel Elizabethen_US
dc.relation.journalThe Journal of Bone & Joint Surgeryen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsMiller, R. E.; Grodzinsky, A. J.; Barrett, M. F.; Hung, H.-H.; Frank, E. H.; Werpy, N. M.; McIlwraith, C. W.; Frisbie, D. D.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8911-7998
dc.identifier.orcidhttps://orcid.org/0000-0002-4942-3456
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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